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Wyszukujesz frazę "Oleszczuk, Marta" wg kryterium: Autor


Wyświetlanie 1-2 z 2
Tytuł:
Cyclic enkephalin-deltorphin hybrids containing a carbonyl bridge: structure and opioid activity
Autorzy:
Ciszewska, Małgorzata
Ruszczyńska, Katarzyna
Oleszczuk, Marta
Chung, Nga
Witkowska, Ewa
Schiller, Peter
Wójcik, Jacek
Izdebski, Jan
Powiązania:
https://bibliotekanauki.pl/articles/1039922.pdf
Data publikacji:
2011
Wydawca:
Polskie Towarzystwo Biochemiczne
Tematy:
cyclic opioid peptides
conformation
NMR
N-(ureidoethyl)amides
side-chain to side-chain cyclization
structure-activity relationship
Opis:
Six hybrid N-ureidoethylamides of octapeptides in which an N-terminal cyclic structure related to enkephalin was elongated by a C-terminal fragment of deltorphin were synthesized on MBHA resin. The synthetic procedure involved deprotection of Boc groups with HCl/dioxane and cleavage of the peptide resin with 45 % TFA in DCM. d-Lys and d-Orn were incorporated in position 2, and Lys, Orn, Dab, or Dap in position 5. The side chains of the dibasic amino function were protected with the Fmoc group. This protection was removed by treatment with 55 % piperidine in DMF, and cyclization was achieved by treatment with bis-(4-nitrophenyl)carbonate. Using various combinations of dibasic amino acids, peptides containing a 17-, 18-, 19- or 20-membered ring structure were obtained. The peptides were tested in the guinea-pig ileum (GPI) and mouse vas deferens (MVD) assays. Diverse opioid activities were observed, depending on the size of the ring. Extension of the enkephalin sequence at the C-terminus by a deltorphin fragment resulted in a change of receptor selectivity in favor of the δ receptor. The conformational propensities of selected peptides were determined using the EDMC method in conjunction with data derived from NMR experiments carried out in water. This approach allowed proper examination of the dynamical behavior of these small peptides. The results were compared with those obtained earlier with corresponding N-(ureidoethyl)pentapeptide amides.
Źródło:
Acta Biochimica Polonica; 2011, 58, 2; 225-230
0001-527X
Pojawia się w:
Acta Biochimica Polonica
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Solution structure of conformationally restricted vasopressin analogues.
Autorzy:
Trzepałka, Emilia
Oleszczuk, Marta
Maciejczyk, Maciej
Lammek, Bernard
Powiązania:
https://bibliotekanauki.pl/articles/1043316.pdf
Data publikacji:
2004
Wydawca:
Polskie Towarzystwo Biochemiczne
Tematy:
vasopressin
X-PLOR
NMR spectroscopy
EDMC
peptide conformation
Opis:
In recent years, a massive effort has been directed towards designing potent and selective antagonists of neurohypophyseal hormones substituted at position 3. Modification of vasopressin at position 3 with 4,4'-biphenylalanine results in pharmacologically inactive analogues. Chemically, this substitution appears to vary only slightly from those previously made by us (1-Nal or 2-Nal), which afforded potent agonists of V2 receptors. In this situation, it seemed worthwhile to study the structure of the analogues with 4,4'-biphenylalanine (BPhe) at position 3 in aqueous solution using NMR spectroscopy and total conformational analysis. This contribution is part of extensive studies aimed at understanding spatial structures of 3-substituted [Arg8]vasopressin analogues of different pharmacological properties. NMR data were used to calculate 3D structures for all the analogues using two methods, EDMC with the ECEPP/3 force field, and molecular dynamic with the simulated annealing (SA) algorithm. The structures obtained by the first method show a better fit between the NMR spectral evidence and the calculation for all the peptides.
Źródło:
Acta Biochimica Polonica; 2004, 51, 1; 33-49
0001-527X
Pojawia się w:
Acta Biochimica Polonica
Dostawca treści:
Biblioteka Nauki
Artykuł
    Wyświetlanie 1-2 z 2

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